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促甲状腺激素释放激素类似物对大鼠大脑中动脉闭塞所致脑缺血的影响。

The effects of TRH analogues on cerebral ischaemia produced by middle cerebral artery occlusion in the rat.

作者信息

Shrewsbury-Gee J, Lye R H, Latham A, Slater P

机构信息

Department of Physiological Sciences, University of Manchester, U.K.

出版信息

Exp Brain Res. 1988;70(2):342-50. doi: 10.1007/BF00248359.

Abstract

This study examined the effects of two stabilised analogues of TRH, RX 77368 and CG 3509, in a rat cerebral ischaemia model produced by unilateral occlusion of the middle cerebral artery. The analogues were given intraventricularly after artery occlusion. The extent of the cortical ischaemia was evaluated after 10 days by somatosensory evoked potential (SEP) recording, followed by tetrazolium staining of brain slices for NADH-diaphorase activity. RX 77368 (2 X 10 micrograms; 15 min, 24 h) significantly improved the survival rate, protected the SEP and reduced the area of infarct. In contrast, neither a smaller dose of RX 77368 (2 X 3 micrograms) nor a 4 h delay in the treatment had any significant beneficial effects. Although CG 3509 (2 X 10 micrograms) resulted in an apparent improvement in survival, its overall effects were not statistically significant. The findings indicate that stabilised TRH analogues may have beneficial effects when given to animals with focal cerebral ischaemia.

摘要

本研究在大脑中动脉单侧闭塞所致的大鼠脑缺血模型中,检测了促甲状腺激素释放激素(TRH)的两种稳定类似物RX 77368和CG 3509的作用。在动脉闭塞后经脑室内给予这些类似物。10天后,通过体感诱发电位(SEP)记录评估皮质缺血程度,随后对脑切片进行四氮唑染色以检测NADH - 黄递酶活性。RX 77368(2×10微克;15分钟,24小时)显著提高了存活率,保护了SEP并减小了梗死面积。相比之下,较小剂量的RX 77368(2×3微克)或治疗延迟4小时均未产生任何显著的有益效果。尽管CG 3509(2×10微克)使存活率有明显提高,但其总体效果无统计学意义。这些发现表明,稳定的TRH类似物给予局灶性脑缺血动物时可能具有有益作用。

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